CA2335941A1 - Treatment of hyperproliferative disorders - Google Patents
Treatment of hyperproliferative disorders Download PDFInfo
- Publication number
- CA2335941A1 CA2335941A1 CA002335941A CA2335941A CA2335941A1 CA 2335941 A1 CA2335941 A1 CA 2335941A1 CA 002335941 A CA002335941 A CA 002335941A CA 2335941 A CA2335941 A CA 2335941A CA 2335941 A1 CA2335941 A1 CA 2335941A1
- Authority
- CA
- Canada
- Prior art keywords
- pharmaceutically acceptable
- acceptable salt
- ceramide
- inhibitor
- subject
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
- A61K31/07—Retinol compounds, e.g. vitamin A
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S424/00—Drug, bio-affecting and body treating compositions
- Y10S424/15—Suppositories
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Steroid Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
A method of treating a hyperproliferative disorder in a subject in need of such treatment, comprising administering to said subject, in combination, a treatment effective amount of: (a) a ceramide-generating retinoid such as fenretinide or a pharmaceutically acceptable salt thereof; and (b) at least one (and in certain embodiments at least two) ceramide degredation inhibitor , such as compounds selected from the group consisting of (i) glucosylceramide synthesis inhibitors, (ii) sphingosine-1-phosphate synthesis inhibitors, and (iii) protein kinase C inhibitors. A preferred glucosyl ceramide synthesis inhibitor is 1-phenyl-2-palmitoylamino-3-morpholino-1-propanol. A preferred sphingosine-1-phosphate synthesis inhibitor is D-erytho-N,N- dimethylsphingosine. A preferred protein kinase C inhibitor is L-threo- dihydrosphingosine.
Claims (33)
1. A method of treating a hyperproliferative disorder in a subject in need of such treatment, comprising administering to said subject, in combination, a treatment effective amount of:
(a) a ceramide-generating retinoid or a pharmaceutically acceptable salt thereof; and (b) a ceramide degradation inhibitor or a pharmaceutically acceptable salt thereof.
(a) a ceramide-generating retinoid or a pharmaceutically acceptable salt thereof; and (b) a ceramide degradation inhibitor or a pharmaceutically acceptable salt thereof.
2. A method according to claim 1, wherein said ceramide degradation inhibitor is selected from the group consisting of glucosyl ceramide synthase inhibitors, sphingosine-1-phosphate synthesis inhibitors, protein kinase C
inhibitors, and the pharmaceutically acceptable salts thereof.
inhibitors, and the pharmaceutically acceptable salts thereof.
3. A method according to claim 1, wherein said hyperproliferative disorder is selected from the group consisting of malignant, pre-malignant, and non-malignant hyperproliferative disorders.
4. A method of treating a hyperproliferative disorder in a subject in need of such treatment, comprising administering to said subject, in combination, a treatment effective amount of:
(a) a ceramide-generating retinoid or a pharmaceutically acceptable salt thereof; and (b) a glucosylceramide synthesis inhibitor or a pharmaceutically acceptable salt thereof.
(a) a ceramide-generating retinoid or a pharmaceutically acceptable salt thereof; and (b) a glucosylceramide synthesis inhibitor or a pharmaceutically acceptable salt thereof.
5. A method according to claim 4, wherein said ceramide-generating retinoid is fenretinide or a pharmaceutically acceptable salt thereof.
6. A method according to claim 4, wherein said glucosylceramide synthesis inhibitor is a glucosylceramide synthase inhibitor or a pharmaceutically acceptable salt thereof.
7. A method according to claim 4, wherein said glucosyl ceramide synthesis inhibitor is 1-phenyl-2-palmitoylamino-3-morpholino-1-propanol or a pharmaceutically acceptable salt thereof.
8. A method of treating a hyperproliferative disorder in a subject in need of such treatment, comprising administering to said subject, in combination, a treatment effective amount of:
(a) a ceramide generating retinoid or a pharmaceutically acceptable salt thereof; and (b) a sphingosine-1-phosphate synthesis inhibitor or a pharmaceutically acceptable salt thereof.
(a) a ceramide generating retinoid or a pharmaceutically acceptable salt thereof; and (b) a sphingosine-1-phosphate synthesis inhibitor or a pharmaceutically acceptable salt thereof.
9. A method according to claim 8, wherein said ceramide-generating retinoid is fenretinide or a pharmaceutically acceptable salt thereof.
10. A method according to claim 8, wherein said sphingosine-1-phosphate synthesis inhibitor is a sphingosine kinase inhibitor or a pharmaceutically acceptable salt thereof.
11. A method according to claim 8, wherein said sphingosine-1-phosphate synthesis inhibitor is D-erythro-N,N-dimethylsphingosine or a pharmaceutically acceptable salt thereof.
12. A method of treating a hyperproliferative disorder in a subject in need of such treatment, comprising administering to said subject, in combination, a treatment effective amount of:
(a) a cermide-generating retinoid or a pharmaceutically acceptable salt thereof;
and (b) a protein kinase C inhibitor or a pharmaceutically acceptable salt thereof.
(a) a cermide-generating retinoid or a pharmaceutically acceptable salt thereof;
and (b) a protein kinase C inhibitor or a pharmaceutically acceptable salt thereof.
13. A method according to claim 12, wherein said ceramide-generating retinoid is fenretinide or a pharmaceutically acceptable salt thereof.
14. A method according to claim 12, wherein said protein kinase C inhibitor is L-threo-dihydrosphingosine or a pharmaceutically acceptable salt thereof.
15. A method of treating a hyperproliferative disorder in a subject in need of such treatment, comprising administering to said subject, in combination, a treatment effective amount of:
(a) a ceramide-generating retinoid or a pharmaceutically acceptable salt thereof; and (b) at least two compounds selected from the group consisting of (i) glucosylceramide synthesis inhibitors and the pharmaceutically acceptable salts thereof, (ii) sphingosine-1-phosphate synthesis inhibitors and the pharmaceutically acceptable salts thereof, and (iii) protein kinase C inhibitors and the pharmaceutically acceptable salts thereof.
(a) a ceramide-generating retinoid or a pharmaceutically acceptable salt thereof; and (b) at least two compounds selected from the group consisting of (i) glucosylceramide synthesis inhibitors and the pharmaceutically acceptable salts thereof, (ii) sphingosine-1-phosphate synthesis inhibitors and the pharmaceutically acceptable salts thereof, and (iii) protein kinase C inhibitors and the pharmaceutically acceptable salts thereof.
16. A method according to claim 15, wherein said ceramide generating retinoid is fenretinide or a pharmaceutically acceptable salt thereof.
17. A method according to claim 15, wherein said at least two compounds comprise (i) a glucosylceramide synthesis inhibitor or a pharmaceutically acceptable salt thereof and (ii) either a sphingosine-1-phosphate synthesis inhibitor, a protein kinase C inhibitor, or a pharmaceutically acceptable salt thereof.
18. A method according to claim 15, wherein said at least two compounds comprise a glucosylceramide synthesis inhibitor or a pharmaceutically acceptable salt thereof, and a sphingosine-1-phosphate synthesis inhibitor or a pharmaceutically acceptable salt thereof.
19. A method according to claim 15, wherein said at least two compounds comprise a glucosylceramide synthesis inhibitor or a pharmaceutically acceptable salt thereof, and a protein kinase C inhibitor or a pharmaceutically acceptable salt thereof.
20. A method according to claim 15, wherein said at least two compounds comprise a sphingosine-1-phosphate synthesis inhibitor or a pharmaceutically acceptable salt thereof, and a protein kinase C inhibitor or a pharmaceutically acceptable salt thereof.
21. A method according to claim 15, wherein said at least two compounds comprise a glucosylceramide synthesis inhibitor or a pharmaceutically acceptable salt thereof, a sphingosine-1-phosphate synthesis inhibitor or a pharmaceutically acceptable salt thereof, and a protein kinase C inhibitor or a pharmaceutically acceptable salt thereof.
22. A method of screening for compounds that increase the cytostatic or cytotoxic activity of a ceramide-generating retinoid in hyperproliferative cells, said method comprising:
(a) contacting first control hyperproliferative cells with an amount of ceramide-generating retinoid;
(b) contacting second control hyperproliferative cells with an amount of a test compound; and (c) contacting experimental hyperproliferative cells with both said amount of ceramide generating retinoid in step (a) above and said amount of a test compound in step (b) above; and (d) determining the growth inhibition of said hyperproliferative cells of steps (a), (b) and (c) above; and then (e) comparing the growth inhibition in the experimental hyperproliferative cells of step (c) with the growth inhibition of the control hyperproliferative cells of steps (a) and (b), a greater degree of growth inhibition determined in the experimental hyperproliferative cells of step (c) than the combined growth inhibition of the control hyperproliferative cells of steps (b) and (c) indicating that the test compound enhances the activity of the ceramide-generating retinoid.
(a) contacting first control hyperproliferative cells with an amount of ceramide-generating retinoid;
(b) contacting second control hyperproliferative cells with an amount of a test compound; and (c) contacting experimental hyperproliferative cells with both said amount of ceramide generating retinoid in step (a) above and said amount of a test compound in step (b) above; and (d) determining the growth inhibition of said hyperproliferative cells of steps (a), (b) and (c) above; and then (e) comparing the growth inhibition in the experimental hyperproliferative cells of step (c) with the growth inhibition of the control hyperproliferative cells of steps (a) and (b), a greater degree of growth inhibition determined in the experimental hyperproliferative cells of step (c) than the combined growth inhibition of the control hyperproliferative cells of steps (b) and (c) indicating that the test compound enhances the activity of the ceramide-generating retinoid.
23. A method according to claim 22, wherein said comparing step is carried out calculating a Combination Index.
24. A method according to claim 22, wherein said hyperproliferative cells are tumor cells.
25. A method according to claim 23, wherein said tumor cells are selected from the group consisting of neuroblastoma, lung, melanoma, prostate, colon, breast.
leukemia and pancreas tumor cells.
leukemia and pancreas tumor cells.
26. A method according to claim 22, wherein said ceramide-generating retinoid is fenretinide or a pharmaceutically acceptable salt thereof.
27. A method according to claim 22, wherein said test compound is a ceramide-degradation inhibitor or a pharmaceutically acceptable salt thereof.
28. A method according to claim 22, wherein said step of determining growth inhibition is carried out by determining necrosis, apoptosis, or both.
29. A compound that increases the cytostatic or cytotoxic activity of a ceramide-generating retinoid in hyperproliferative cells produced by the method of claim 22, or a pharmaceutically acceptable salt thereof.
30. A pharmaceutical formulation comprising, in a pharmaceutically acceptable carrier, a treatment effective amount of a compound that increases the cytostatic or cytotoxic activity of a ceramide-generating retinoid in hyperproliferative cells produced by the method of claim 22, or a pharmaceutically acceptable salt thereof.
31. A pharmaceutical formulation according to claim 31, further comprising a treatment effective amount of a ceramide generating retinoid or a pharmaceutically acceptable salt thereof.
32. A method of treating a hyperproliferative disorder in a subject in need of such treatment, comprising administering to said subject, in combination, a treatment effective amount of:
(a) a ceramide-generating retinoid or a pharmaceutically acceptable salt thereof; and (b) a compound that increases the cytostatic or cytotoxic activity of a ceramide-generating retinoid in hyperproliferative cells produced by the method of claim 22, or a pharmaceutically acceptable salt thereof.
(a) a ceramide-generating retinoid or a pharmaceutically acceptable salt thereof; and (b) a compound that increases the cytostatic or cytotoxic activity of a ceramide-generating retinoid in hyperproliferative cells produced by the method of claim 22, or a pharmaceutically acceptable salt thereof.
33. A method according to claim 32, wherein said hyperproliferative disorder is selected from the group consisting of malignant, pre-malignant, and non-malignant hyperproliferative disorders.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9113898P | 1998-06-29 | 1998-06-29 | |
| US60/091,138 | 1998-06-29 | ||
| PCT/US1999/014591 WO2000000207A1 (en) | 1998-06-29 | 1999-06-28 | Treatment of hyperproliferative disorders |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2335941A1 true CA2335941A1 (en) | 2000-01-06 |
| CA2335941C CA2335941C (en) | 2011-03-22 |
Family
ID=22226266
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2335941A Expired - Lifetime CA2335941C (en) | 1998-06-29 | 1999-06-28 | Treatment of hyperproliferative disorders |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US6352844B1 (en) |
| EP (1) | EP1091745B1 (en) |
| JP (1) | JP4965764B2 (en) |
| CN (1) | CN100358529C (en) |
| AT (1) | ATE409486T1 (en) |
| AU (1) | AU4724599A (en) |
| BR (1) | BR9912501A (en) |
| CA (1) | CA2335941C (en) |
| DE (1) | DE69939651D1 (en) |
| DK (1) | DK1091745T3 (en) |
| ES (1) | ES2316188T3 (en) |
| WO (1) | WO2000000207A1 (en) |
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| US6098631A (en) * | 1998-01-21 | 2000-08-08 | The Regents Of The University Of Michigan | Compositions and methods for treating autoimmune disease |
| US6368831B1 (en) * | 1998-06-29 | 2002-04-09 | Childrens Hospital Los Angeles | Treatment of hyperproliferative disorders |
| GB0006539D0 (en) * | 2000-03-17 | 2000-05-10 | Oxford Glycosciences Uk Ltd | Therapies |
| AUPQ744700A0 (en) * | 2000-05-11 | 2000-06-01 | Medvet Science Pty. Ltd. | A method of treatment and agents useful for same |
| EP1195604A1 (en) | 2000-09-29 | 2002-04-10 | Warner-Lambert Company | Methods and compositions for screening modulators of lipid kinases |
| WO2002058689A1 (en) * | 2000-12-05 | 2002-08-01 | Childrens Hospital Los Angeles | Pharmaceutical compositions of fenretinide having increased bioavailability and methods of using the same |
| EP1363643A2 (en) * | 2000-12-22 | 2003-11-26 | Medlyte, Inc. | Compositions and methods for the treatment and prevention of cardiovascular diseases and disorders, and for identifying agents therapeutic therefor |
| US20040097587A1 (en) * | 2002-03-27 | 2004-05-20 | Arbiser Jack L | Compositions and methods of treatment of ulcerating diseases, burns, and related conditions |
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| JP3405981B1 (en) * | 2002-06-26 | 2003-05-12 | 日本財経株式会社 | Method for producing cellulose acetate |
| AU2002357644A1 (en) * | 2002-09-20 | 2004-04-08 | Medisyn Technologies, Inc. | Therapeutic agents and corresponding treatments |
| EP1594544B1 (en) * | 2003-01-31 | 2016-04-06 | Childrens Hospital Los Angeles | Oral compositions of fenretinide having increased bioavailability and methods of using the same |
| DE602004001393T2 (en) * | 2003-02-21 | 2007-06-14 | Childrens Hospital of Los Angeles Research Institute, Los Angeles | STABLE PHARMACEUTICAL COMPOSITION WITH SAFINGOL AND METHOD FOR THE USE THEREOF |
| US20050101674A1 (en) * | 2003-11-12 | 2005-05-12 | Maurer Barry J. | PPMP as a ceramide catabolism inhibitor for cancer treatment |
| WO2005072091A2 (en) * | 2003-12-09 | 2005-08-11 | The Government Of The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services | Methods for inhibiting hiv and other viral infections by modulating ceramide metabolism |
| US7754769B2 (en) | 2004-03-02 | 2010-07-13 | Mcgill University | Compositions and methods for preventing or treating an inflammatory response |
| US7794713B2 (en) * | 2004-04-07 | 2010-09-14 | Lpath, Inc. | Compositions and methods for the treatment and prevention of hyperproliferative diseases |
| US20090111812A1 (en) * | 2004-06-14 | 2009-04-30 | Musc Foundation For Research Development | Methods for treating inflammatory disorders |
| WO2006010127A2 (en) * | 2004-07-09 | 2006-01-26 | Medisyn Technologies, Inc. | Therapeutic compound and treatments |
| ES2410866T3 (en) * | 2004-10-28 | 2013-07-03 | Lpath, Inc. | Compositions and procedures for the treatment and prevention of hyperproliferative diseases |
| US20060257493A1 (en) * | 2005-04-28 | 2006-11-16 | Amiji Mansoor M | Nanoparticulate delivery systems for treating multi-drug resistance |
| US20090074720A1 (en) * | 2005-10-28 | 2009-03-19 | Sabbadini Roger A | Methods for decreasing immune response and treating immune conditions |
| US20080213274A1 (en) * | 2005-10-28 | 2008-09-04 | Sabbadini Roger A | Compositions and methods for the treatment and prevention of fibrotic, inflammatory, and neovascularization conditions of the eye |
| NZ572601A (en) | 2006-03-29 | 2012-03-30 | Univ Wayne State | Liposomal nanoparticles and other formulations of fenretinide for use in therapy and drug delivery |
| US9274129B2 (en) * | 2006-05-31 | 2016-03-01 | Lpath, Inc. | Methods and reagents for detecting bioactive lipids |
| US8796429B2 (en) * | 2006-05-31 | 2014-08-05 | Lpath, Inc. | Bioactive lipid derivatives, and methods of making and using same |
| US7862812B2 (en) * | 2006-05-31 | 2011-01-04 | Lpath, Inc. | Methods for decreasing immune response and treating immune conditions |
| US9274130B2 (en) | 2006-05-31 | 2016-03-01 | Lpath, Inc. | Prevention and treatment of pain using antibodies to lysophosphatidic acid |
| US9217749B2 (en) * | 2006-05-31 | 2015-12-22 | Lpath, Inc. | Immune-derived moieties reactive against lysophosphatidic acid |
| US8444970B2 (en) * | 2006-10-27 | 2013-05-21 | Lpath, Inc. | Compositions and methods for treating ocular diseases and conditions |
| SI2087002T1 (en) | 2006-10-27 | 2014-11-28 | Lpath, Inc. | Compositions and methods for binding sphingosine-1-phosphate |
| US20100311765A1 (en) * | 2007-09-28 | 2010-12-09 | Barry James Maurer | Metabolic degradation inhibitors for anti-hyperproliferative agents |
| US8361465B2 (en) * | 2007-10-26 | 2013-01-29 | Lpath, Inc. | Use of anti-sphingosine-1-phosphate antibodies in combination with chemotherapeutic agents |
| GB0803352D0 (en) | 2008-02-22 | 2008-04-02 | Ntnu Technology Transfer As | Oligopeptidic compounds and uses thereof |
| US20090253733A1 (en) * | 2008-04-02 | 2009-10-08 | Biointeractions, Ltd. | Rapamycin carbonate esters |
| CN101623277B (en) * | 2008-07-08 | 2014-07-16 | 上海交通大学医学院附属瑞金医院 | New application of fenretinide and active derivatives thereof and pharmaceutical composition of fenretinide and active derivatives thereof |
| US8088822B2 (en) * | 2008-07-08 | 2012-01-03 | Ji Zhang | Use of fenretinide or bioactive derivatives thereof and pharmaceutical compositions comprising the same |
| US8871202B2 (en) | 2008-10-24 | 2014-10-28 | Lpath, Inc. | Prevention and treatment of pain using antibodies to sphingosine-1-phosphate |
| EP2669267B1 (en) * | 2009-11-12 | 2018-01-10 | Texas Tech University | Compositions and methods for treating hyperproliferative disorders |
| US8450350B2 (en) * | 2010-05-05 | 2013-05-28 | Infinity Pharmaceuticals, Inc. | Triazoles as inhibitors of fatty acid synthase |
| WO2012068169A2 (en) * | 2010-11-15 | 2012-05-24 | Texas Tech University | Substance for increasing the production of a specific acyl-chain dihydroceramide(s) for improving the effectiveness of cancer treatments |
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-
1999
- 1999-06-28 EP EP99930790A patent/EP1091745B1/en not_active Expired - Lifetime
- 1999-06-28 AU AU47245/99A patent/AU4724599A/en not_active Abandoned
- 1999-06-28 ES ES99930790T patent/ES2316188T3/en not_active Expired - Lifetime
- 1999-06-28 US US09/342,019 patent/US6352844B1/en not_active Expired - Lifetime
- 1999-06-28 DK DK99930790T patent/DK1091745T3/en active
- 1999-06-28 JP JP2000556792A patent/JP4965764B2/en not_active Expired - Lifetime
- 1999-06-28 AT AT99930790T patent/ATE409486T1/en not_active IP Right Cessation
- 1999-06-28 CA CA2335941A patent/CA2335941C/en not_active Expired - Lifetime
- 1999-06-28 BR BR9912501-3A patent/BR9912501A/en not_active IP Right Cessation
- 1999-06-28 WO PCT/US1999/014591 patent/WO2000000207A1/en active Application Filing
- 1999-06-28 CN CNB998081426A patent/CN100358529C/en not_active Expired - Fee Related
- 1999-06-28 DE DE69939651T patent/DE69939651D1/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EP1091745A1 (en) | 2001-04-18 |
| WO2000000207A9 (en) | 2000-05-18 |
| CA2335941C (en) | 2011-03-22 |
| AU4724599A (en) | 2000-01-17 |
| JP4965764B2 (en) | 2012-07-04 |
| EP1091745A4 (en) | 2003-08-27 |
| WO2000000207A1 (en) | 2000-01-06 |
| DK1091745T3 (en) | 2008-12-15 |
| CN100358529C (en) | 2008-01-02 |
| DE69939651D1 (en) | 2008-11-13 |
| CN1308538A (en) | 2001-08-15 |
| ES2316188T3 (en) | 2009-04-01 |
| BR9912501A (en) | 2001-05-02 |
| JP2002519329A (en) | 2002-07-02 |
| EP1091745B1 (en) | 2008-10-01 |
| ATE409486T1 (en) | 2008-10-15 |
| US6352844B1 (en) | 2002-03-05 |
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